Skip to content

LGR5 expression is regulated by EGF in early colorectal adenomas and governs EGFR inhibitor sensitivity

Research output: Contribution to journalArticle

Standard

LGR5 expression is regulated by EGF in early colorectal adenomas and governs EGFR inhibitor sensitivity. / Morgan, R G; Mortensson, E; Legge, D N; Gupta, B; Collard, T J; Greenhough, A; Williams, Ann C.

In: British Journal of Cancer, Vol. 118, No. 4, 20.02.2018, p. 558-565.

Research output: Contribution to journalArticle

Harvard

APA

Vancouver

Morgan RG, Mortensson E, Legge DN, Gupta B, Collard TJ, Greenhough A et al. LGR5 expression is regulated by EGF in early colorectal adenomas and governs EGFR inhibitor sensitivity. British Journal of Cancer. 2018 Feb 20;118(4):558-565. https://doi.org/10.1038/bjc.2017.412

Author

Morgan, R G ; Mortensson, E ; Legge, D N ; Gupta, B ; Collard, T J ; Greenhough, A ; Williams, Ann C. / LGR5 expression is regulated by EGF in early colorectal adenomas and governs EGFR inhibitor sensitivity. In: British Journal of Cancer. 2018 ; Vol. 118, No. 4. pp. 558-565.

Bibtex

@article{5da99d41043c4f19b24926ab9ddeef49,
title = "LGR5 expression is regulated by EGF in early colorectal adenomas and governs EGFR inhibitor sensitivity",
abstract = "BACKGROUND: LGR5 serves as a co-receptor for Wnt/β-catenin signalling and marks normal intestinal stem cells; however, its role in colorectal cancer (CRC) remains controversial. LGR5(+) cells are known to exist outside the stem cell niche during CRC progression, and the requirement for epidermal growth factor (EGF) signalling within early adenomas remains to be fully elucidated.METHODS: Epidermal growth factor and gefitinib treatments were performed in EGF-responsive LGR5(+) early adenoma RG/C2 cells. 2D growth assays were measured using an IncuCyte. LGR5 or MEK1/2 silencing studies were executed using siRNA and LGR5 expression was assessed by qRT-PCR and immunoblotting. Ki67 level and cell cycle status were analysed by flow cytometry.RESULTS: Epidermal growth factor suppresses expression of LGR5 at both the transcript and protein level in colorectal adenoma and carcinoma cells. Suppression of LGR5 reduces the survival of EGF-treated adenoma cells by increasing detached cell yield but also inducing a proliferative state, as evidenced by elevated Ki67 level and enhanced cell cycle progression. Repression of LGR5 further increases the sensitivity of adenoma cells to EGFR inhibition.CONCLUSIONS: LGR5 has an important role in the EGF-mediated survival and proliferation of early adenoma cells and could have clinical utility in predicting response of CRC patients to EGFR therapy.British Journal of Cancer advance online publication, 16 November 2017; doi:10.1038/bjc.2017.412 www.bjcancer.com.",
keywords = "LGR5, EGF, colorectal, adenoma, proliferation, survival, EGFRi, gefitinib",
author = "Morgan, {R G} and E Mortensson and Legge, {D N} and B Gupta and Collard, {T J} and A Greenhough and Williams, {Ann C}",
year = "2018",
month = "2",
day = "20",
doi = "10.1038/bjc.2017.412",
language = "English",
volume = "118",
pages = "558--565",
journal = "British Journal of Cancer",
issn = "0007-0920",
publisher = "Springer Nature",
number = "4",

}

RIS - suitable for import to EndNote

TY - JOUR

T1 - LGR5 expression is regulated by EGF in early colorectal adenomas and governs EGFR inhibitor sensitivity

AU - Morgan, R G

AU - Mortensson, E

AU - Legge, D N

AU - Gupta, B

AU - Collard, T J

AU - Greenhough, A

AU - Williams, Ann C

PY - 2018/2/20

Y1 - 2018/2/20

N2 - BACKGROUND: LGR5 serves as a co-receptor for Wnt/β-catenin signalling and marks normal intestinal stem cells; however, its role in colorectal cancer (CRC) remains controversial. LGR5(+) cells are known to exist outside the stem cell niche during CRC progression, and the requirement for epidermal growth factor (EGF) signalling within early adenomas remains to be fully elucidated.METHODS: Epidermal growth factor and gefitinib treatments were performed in EGF-responsive LGR5(+) early adenoma RG/C2 cells. 2D growth assays were measured using an IncuCyte. LGR5 or MEK1/2 silencing studies were executed using siRNA and LGR5 expression was assessed by qRT-PCR and immunoblotting. Ki67 level and cell cycle status were analysed by flow cytometry.RESULTS: Epidermal growth factor suppresses expression of LGR5 at both the transcript and protein level in colorectal adenoma and carcinoma cells. Suppression of LGR5 reduces the survival of EGF-treated adenoma cells by increasing detached cell yield but also inducing a proliferative state, as evidenced by elevated Ki67 level and enhanced cell cycle progression. Repression of LGR5 further increases the sensitivity of adenoma cells to EGFR inhibition.CONCLUSIONS: LGR5 has an important role in the EGF-mediated survival and proliferation of early adenoma cells and could have clinical utility in predicting response of CRC patients to EGFR therapy.British Journal of Cancer advance online publication, 16 November 2017; doi:10.1038/bjc.2017.412 www.bjcancer.com.

AB - BACKGROUND: LGR5 serves as a co-receptor for Wnt/β-catenin signalling and marks normal intestinal stem cells; however, its role in colorectal cancer (CRC) remains controversial. LGR5(+) cells are known to exist outside the stem cell niche during CRC progression, and the requirement for epidermal growth factor (EGF) signalling within early adenomas remains to be fully elucidated.METHODS: Epidermal growth factor and gefitinib treatments were performed in EGF-responsive LGR5(+) early adenoma RG/C2 cells. 2D growth assays were measured using an IncuCyte. LGR5 or MEK1/2 silencing studies were executed using siRNA and LGR5 expression was assessed by qRT-PCR and immunoblotting. Ki67 level and cell cycle status were analysed by flow cytometry.RESULTS: Epidermal growth factor suppresses expression of LGR5 at both the transcript and protein level in colorectal adenoma and carcinoma cells. Suppression of LGR5 reduces the survival of EGF-treated adenoma cells by increasing detached cell yield but also inducing a proliferative state, as evidenced by elevated Ki67 level and enhanced cell cycle progression. Repression of LGR5 further increases the sensitivity of adenoma cells to EGFR inhibition.CONCLUSIONS: LGR5 has an important role in the EGF-mediated survival and proliferation of early adenoma cells and could have clinical utility in predicting response of CRC patients to EGFR therapy.British Journal of Cancer advance online publication, 16 November 2017; doi:10.1038/bjc.2017.412 www.bjcancer.com.

KW - LGR5

KW - EGF

KW - colorectal

KW - adenoma

KW - proliferation

KW - survival

KW - EGFRi

KW - gefitinib

U2 - 10.1038/bjc.2017.412

DO - 10.1038/bjc.2017.412

M3 - Article

VL - 118

SP - 558

EP - 565

JO - British Journal of Cancer

JF - British Journal of Cancer

SN - 0007-0920

IS - 4

ER -